FDA recall D-0216-2018

SHISEIDO AMERICA INC. · Class II · drug

Product

Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%, octocrylebe 3.0%, oxybenzone 1.0% and zinc oxide 15.4%), packaged in 15 mL tubes, Shiseido Americas Corporation Dist. New York, NY 10022,

Reason for recall

GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.

Distribution

Product was distributed nationwide.

Key facts

Status
Terminated
Initiation date
2017-12-14
Report date
2018-01-24
Termination date
2021-06-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
East Windsor, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0216-2018